HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 2-[N-tert-butoxycarbonyl-N-(2'-carbamoylbiphenyl-4-yl)methylamino]-3-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate | HCID 9965968 | — |
| Reactant | 4'-(Bromomethyl)-[1,1'-biphenyl]-2-carboxamide | HCID 15219006 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-[N-tert-butoxycarbonyl-N-(2'-carbamoylbiphenyl-4-yl)methylamino]-3-nitrobenzoate | HCID 54203098 | 90% |
Reaction Steps
A mixture of methyl 2-(N-tert-butoxycarbonylamino)-3-nitrobenzoate (1.8 g), 4'-bromomethylbiphenyl-2-carboxamide (1.8 g) and K2CO3 (0.86 g) in acetonitrile (25 ml) was heated for 6 hours under reflux. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over MgSO4. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica gel to afford a yellow syrup (2.3 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05243054 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-71fc841a6d9944a2bee1d36da445a3d0 |
| Source note | uspto-grants-1993_09 |